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Dr Samantha Carlson is an early career mixed-methods social scientist, leading research that seeks to understand how to improve access to and understanding about vaccination.

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After 20 years at the Institute, Hannah’s career has been a whirlwind of discovery and dedication.

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The Together magazine shines a light on our community. It's our way to say thanks to those who tirelessly fundraise or volunteer, to those who donate, advocate, participate in and help drive child health research.

We hypothesised that MECP2 mutations occur predominantly on the male derived X chromosome.

We wanted to describe the range and variability in the expression of symptoms in girls and women with Rett syndrome.

We compared the symptoms and genetic characteristics of girls with Rett syndrome and both with and without initial diagnosis of autism.

We described the occurrence of scoliosis in Rett syndrome, how it develops and how it is influenced by the individual's age, mutation type, and walking ability.